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QC Analyst

Location: Dublin North, Dublin
Salary: Negotiable
Posted: about 2 months ago
Role type: Permanent
Industry: Science, Technology and Operations Practice (STO), Science Leaders & Specialists
Contact name: Maeve Fahey
Contact email: maeve.fahey@hrmrecruit.com

Job description

This privately owned pharmaceutical organisation have an extensive portfolio of healthcare products and a robust drug development pipeline. They have a product presence in approximately 190 countries worldwide. Due to continued growth and new product introduction, a vacancy has opened up for a QC Analyst to join the team.

The Role

Responsibilities of the QC Analyst include but are not limited to:

  • Analysing raw material, in-process, finished product and stability samples according to specifications, primarily HPLC and dissolution
  • Analysing validation samples according to validation protocols and investigational samples as directed
  • Recording results in a timely and accurate fashion
  • Receiving and logging samples into the Laboratory
  • Ensuring the Right First Time KPI with respect to Analyst's documentation are achieved
  • Troubleshooting any erroneous analytical data obtained
  • Helping to ensure laboratory SOPs and specifications are kept up to date and in a state of compliance

The Person

The ideal candidate will have qualifications & experience in the following:

  • Degree in a Life Science or similar
  • 12 months' work experience working within a pharmaceutical cGLP environment (HPRA and FDA approved) using HPLC, IC & GC testing methods
  • Ability to trouble shoot, identify analytical issues and follow up with corrective actions
  • Knowledge of validation and tech transfers is desirable

To discover more about this opportunity, apply now or contact Maeve Fahey at HRM on +353 1 6321885 for a confidential discussion.

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Maeve Fahey

Science Recruitment Consultant

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